Ketone/Aldehyde → Amine via Reductive Amination (Planning Page): Workflow + Practice
Reductive amination is the most direct way to convert carbonyls to amines: form an imine/iminium, then reduce it selectively.
- Reaction: Ketone/Aldehyde → Amine via Reductive Amination (Planning Page)
- What it does: Reductive amination is the most direct way to convert carbonyls to amines: form an imine/iminium, then reduce it selectively.
- Typical reagents: NaBH3CN, AcOH (or NaBH(OAc)3)
- Key intermediate: Iminium ion
- Driving force: Hydride delivery to electrophile
- Exam type: Choose reagents
- Exam type: Plan order of operations
- Exam type: Chemoselectivity